# Hilma Hólm

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/hilma-holm/

## Facts

| Field | Value |
| --- | --- |
| Citations | 37,264 |
| Field | Genetic Associations and Epidemiology |
| h-index | 79 |
| i10-index | 166 |
| Last Known Institution | deCODE Genetics (Iceland) |
| OpenAlex ID | https://openalex.org/A5084707737 |
| ORCID iD | https://orcid.org/0000-0002-9517-6636 |
| Works | 263 |

## Researcher papers

- [The power of genetic diversity in genome-wide association studies of lipids](https://scholariq.org/papers/the-power-of-genetic-diversity-in-genome-wide-association-studies-of-lipids/)
- [Humoral Immune Response to SARS-CoV-2 in Iceland](https://scholariq.org/papers/humoral-immune-response-to-sars-cov-2-in-iceland/)
- [Variants conferring risk of atrial fibrillation on chromosome 4q25](https://scholariq.org/papers/variants-conferring-risk-of-atrial-fibrillation-on-chromosome-4q25/)
- [Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants](https://scholariq.org/papers/discovery-and-systematic-characterization-of-risk-variants-and-genes-for/)
- [A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke](https://scholariq.org/papers/a-sequence-variant-in-zfhx3-on-16q22-associates-with-atrial-fibrillation-and/)
- [Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels](https://scholariq.org/papers/target-genes-variants-tissues-and-transcriptional-pathways-influencing-human/)
- [Several common variants modulate heart rate, PR interval and QRS duration](https://scholariq.org/papers/several-common-variants-modulate-heart-rate-pr-interval-and-qrs-duration/)
- [Seventy-five genetic loci influencing the human red blood cell](https://scholariq.org/papers/seventy-five-genetic-loci-influencing-the-human-red-blood-cell/)
- [Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density](https://scholariq.org/papers/sequence-variants-in-the-cldn14-gene-associate-with-kidney-stones-and-bone/)
- [Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes](https://scholariq.org/papers/lipoprotein-a-concentration-and-risks-of-cardiovascular-disease-and-diabetes/)
- [Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm](https://scholariq.org/papers/genome-wide-association-study-identifies-a-sequence-variant-within-the-dab2ip/)
- [Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases](https://scholariq.org/papers/association-of-variants-at-umod-with-chronic-kidney-disease-and-kidney-stones/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Metabolomics and Mass Spectrometry Studies](https://scholariq.org/topics/metabolomics-and-mass-spectrometry-studies/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Cardiomyopathy and Myosin Studies](https://scholariq.org/topics/cardiomyopathy-and-myosin-studies/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)

## Researcher university

- [deCODE Genetics (Iceland)](https://scholariq.org/institutions/decode-genetics-iceland/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.